Active Ingredient
Camphor 2%
Nekvnro Medicated Lip Ointment.
FDA Label NDC 84844-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guoyu Trading Co., Ltd. for the product Nekvnro Medicated Lip Ointment. (NDC 84844-004). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, use, warnings, do not use, when using, stop use, ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
External Analgesic
Use
·Helps provide relief of symptoms of cold sores and dry lips.
Warnings
·For external use only. When using this product, keep out of eyes. Rinse with water to remove.
Do Not Use
on deep puncture wounds, serious burns, or animal bites.
When Using
this product, keep out of eyes. Rinse with water to remove.
Stop Use
if the condition worsens or symptoms last more than 7 days or clear up and occur again within a few days
Ask Doctor
if the condition worsens or symptoms last more than 7 days or clear up and occur again within a few days
Keep Oot Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
· Apply to lips not more than 3 to 4 times daily. Children under 2 years of age: ask a doctor.
Other Information
This is a personal care item and should be used by one individual only.Inactive
Inactive Ingredients
·Beeswax white, GLYCERYL 2-CAPRYLATE，Lanolin, Oleamide, Paraffin,Propyl Acetate
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